US2817619A - Process for preparing polyester-faced bodies - Google Patents

Process for preparing polyester-faced bodies Download PDF

Info

Publication number
US2817619A
US2817619A US441152A US44115254A US2817619A US 2817619 A US2817619 A US 2817619A US 441152 A US441152 A US 441152A US 44115254 A US44115254 A US 44115254A US 2817619 A US2817619 A US 2817619A
Authority
US
United States
Prior art keywords
polyester
coating
cured
resin
mold surface
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US441152A
Inventor
David K Bickel
Stephen J Mittl
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Akzo Nobel Paints LLC
Original Assignee
Glidden Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Glidden Co filed Critical Glidden Co
Priority to US441152A priority Critical patent/US2817619A/en
Application granted granted Critical
Publication of US2817619A publication Critical patent/US2817619A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C70/00Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
    • B29C70/04Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising reinforcements only, e.g. self-reinforcing plastics
    • B29C70/06Fibrous reinforcements only
    • B29C70/10Fibrous reinforcements only characterised by the structure of fibrous reinforcements, e.g. hollow fibres
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/007Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by mechanical or physical treatments
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/12Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
    • D06N3/121Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with polyesters, polycarbonates, alkyds
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21JFIBREBOARD; MANUFACTURE OF ARTICLES FROM CELLULOSIC FIBROUS SUSPENSIONS OR FROM PAPIER-MACHE
    • D21J1/00Fibreboard
    • D21J1/16Special fibreboard
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S52/00Static structures, e.g. buildings
    • Y10S52/07Synthetic building materials, reinforcements and equivalents
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249953Composite having voids in a component [e.g., porous, cellular, etc.]
    • Y10T428/249967Inorganic matrix in void-containing component
    • Y10T428/249968Of hydraulic-setting material
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/25Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
    • Y10T428/259Silicic material
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31786Of polyester [e.g., alkyd, etc.]
    • Y10T428/31794Of cross-linked polyester

Definitions

  • Thisinvention relates to a process for preparing bodies composed of or comprising a cured polyester resin mass as a backing on the surface of which is integrally attached an exposed or finish layer of clear or pigmented polyester resin.
  • the invention contemplates the provision of either finish layers of a monotone appearance, or finish layers combining two or more different colors or resinous masses in any desired arrangement or pattern.
  • polyester resins alkyd resins prepared mainly from saturated polyhydric alcohols and ethylenically-unsaturated polycarboxylic acids
  • resinous products which combine polyester resins with polymerizable ethylenically unsaturated monomers
  • Such resinous compositions are, moreover, excellent binders and molding materials and hence can be used prominently in a wide variety of finished products.
  • molded arti cles of excellent mechanical strength can be produced.
  • polyesters and polyestenmonomer combinations are beset with one disadvantage in particular; namely, that to the best of the applicants present knowledge, few known paints, inks, or conventional coating compositions other than cer tain lacquers will adhere satisfactorily to the cured surface of such resinous materials.
  • This quality while advantageous in many respects, is a definite disadvantage from the standpoint of applying markings, legends, insignia, decorations, etc. to cured surfaces of the resins.
  • markings as trademarks, trade names, manufacturers name and address, quality or grade designations, and the like cannot be affixed permanently in any simple manner.
  • Polyester or polyester-monomer resins are currently being used rather extensively in making a variety of reinforced decorative and/or structural materials as automobile bodies, safety helmets, lamp shades, canopy material in corrugated sheet form, light weight bath-tubs for automobile trailers, ⁇ and many other objects. in most instances certain of the reinforcing bers are very close to the surface of the finished objects and in some instances may penetratethe surface. lf the surface is sanded in an ⁇ effort to out o' the protruding reinforcing fibers the very act of abradingthe surface exposes new fiberswhich ⁇ further detract from ⁇ thed'esired smooth, pore-free surface.
  • each exposed reVw inforcing fiber functions as a wick in leading moisture through the cured mass of polyester.
  • glassiiber-reinforced polyester tubing is not watertight because of the wick action of fibers which penetrate through the inner surface of the tubing.
  • Our process involves the concept of building up the desired finished body inwardly from the desired smooth, defect-free outer surface, rather than to build it from the inside out, as has heretofore been attempted.
  • the desired outer surface can be pro vided in the form, quality, color and pattern sought, whether that be a liber-free and pore-free surface of a single homogeneous color, a sign ⁇ exposing an outer surface of two or more colors, or a decorative surface having an appearance and pattern resembling wood, marble, or otherwise.
  • the desired outer surface is provided first of all by applying a selected gelable polyester composition to an appropriate mold surface and then is gelled in place on said mold surface without being cured; then a desired polyester mass reinforced or not can be applied on top thereof and in some instances gelled without being fully cured, and then (if desired) structural and/or reinforcing members of metal, stone, rock, concrete or the like can be applied on top of the gelled but uncured mass.
  • the entire assembly so built up can then be treated to cure the various resin layers simultaneously, as by heat alone, or by combinations of heat and pressure, to give a finished body having ail of the various layers and masses integrally united each to another and to any structural members employed therein, thereby to provide a body having a durable, smooth, glossy, abrasionand chemical-resistant outer surface carrying any desired legends, indicia or patterns as an integral part of that outer surface.
  • Fig. l is a vertical longitudinal sectional view of a building block as positioned in a tray for applying a composite facing thereto;
  • Fig. 2 is a vertical cross-sectional view taken on the line 2 2 of Fig. 1;
  • Fig. 3 is a plan view of a mold for a license plate. showing identifying characters which have been sprayed on the bottom face of the mold by means of a reverse stencil;
  • Fig. 4 is a vertical sectional View of the mold of Fig. 4 as taken on the line 4-4 after additional layers of materials have been provided therein, said view having its vertical dimensions greatly enlarged;
  • Fig. 5 is a plan view of the completed license plate after being ejected from the mold
  • Fig. 6 is a plan view of an assembly such as could be prepared in accordance with the invention in making a decorated sheet of polyester foil;
  • Fig. 7 is a vertical sectional view of the assembly of Fig. 6, taken on the line 7-7 and greatly enlarged in the vertical dimensions.
  • EXAMPLE l Building black faced with polyester' resin
  • This example illustrates the principles of the invention as applied to the preparation of a faced porous building block whose dimensions are approximately 8" x 8" x 16".
  • the object of facing the building block is to provide at least one smooth, non-porous, exposure-resistant facing on the block to present any desired color or color pattern.
  • Such faced blocks can be laid up so as to form a wall presenting their resinfaced surfaces either to an inside room of a structure, or to the weather side of the wall.
  • the blocks may, of course, be faced on both sides.
  • the facings are exposed to the weather, they provide an exterior surface which needs no painting, which is water-tight, which stays clean by reason of its smoothness and weather resistance, and which is rnar resistant by reason of its toughness, abrasion resistance and hardness.
  • the facings are presented to interior rooms of a structure, they alford many of the advantages mentioned above plus ease of cleaning, retention of color, brightness and decorative qualities, excellent durability and a certain degree of fire-resistance.
  • Such a surface seldom needs to be more than a few thousandths of an inch thick but in commercial practice may be as much as 3%000 of an inch thick. Any desired thickness can, of course, be used.
  • outer layer Under the just-described outer layer will be a resinous layer which has been pigmented and/or filled or reinforced with appropriate materials, the pigmentation giving a sub-surface layer of desired hiding qualities with the fillers and reinforcement functioning to extend or bulk the resin while yet providing a strong, dense layer capable of adequately supporting the nonporous exposed surface layer.
  • the intermediate layer must of course be firmly bonded both to the exposed surface layer and to the cinder block.
  • a clean metal tray 1 having dimensions of about 8" x 16" in plan view and about l/.” deep is sprayed to a thickness of about 5 to l0 mils with a catalyzed 100% polymerizable, gelable resinous polyester mass formulated as follows, thereby to provide a layer 2 in the tray.
  • Polyester C liquid ounces.
  • Polyester A is a liquid heathardeuable polyester composition prepared from the following ingredients:
  • Polyesters B and C are similar heat-hardenable cornpositions, formulated as indicated below:
  • Polyester B Lbs. Propylene glycol 29.90 Maleic anhydride 17.50 Adipic acid 26.10 Styrene 27.35 Xylol 5.88 4tertbutyl catechol .009 Choline chloride.l .456 Propylene glycol1 .10
  • polyester compositions can be prepared individually by esterifying the polyhydric alcohol(s) and polycarboxylic acids in the presence of xylol as the iirst step, then the volatiles are stripped olf and, after cooling, the stabilizers and styrene are added. The resulting cornpositions are polymerizable.
  • the sprayed coating is converted in a few minutes to a fairly firm gelled condition at room ternperature, and by adding 1% of benzoyl peroxide or 1% methylethylketone peroxide the sprayed layer 2 can be gelled at 225 F. in about 1 to 3 minutes.
  • a suitable backing-and-bonding mass formulated as follows is then added to the tray in an amount of about 1.5 lbs. to form a layer 3.
  • the mass is catalyzed for curing by incorporating 0.5 %1.0% of methylethylketone peroxide, t-butyl peroxide or benzoyl peroxide.
  • the above backing-and-bonding mass is a thick, creamy material which can be poured into the tray and spread easily therein. It has enough body to carry the weight of the cinder block Without being squeezed out of the tray.
  • the cinder block 4 is then positioned in the tray with. one face thereof resting upon the layer tional backing-and-bonding material can then be intro- ⁇ quizd ⁇ between the edges of the block and the sides of the tray to completely hide the face which is being coated.
  • the tray with its entire assembly is next passed into an oven where the whole unit isheated at 350 F. for about 45 minutes, thereby curing ⁇ the gelled polyester resin layer 2 and the layer 3- of backing-and-bonding mass, and bonding them to each other and to the cinder block. Gn emergence from the oven, the tray 1 can be easily removed from the cured assembly and returned for use in preparing another cured assembly, since the above formulations do not adhere tothe tray after being cured.
  • the first-applied gelled coating 2 cures to a dense, pore-free, smooth surface of desired uniform color and presents the physical and chemical properties of the selected polyester resin as the Wearing face of the block.
  • the second-applied gelled layer 3v is relatively high in pigment and filler and low in resin content and hence of moderate total cost even though being used" in appreciable volume (e. g., about l.5 lbs. per face) to give hiding, bonding, pore-filling, and leveling-out between the first gelled coat and non-flat block faces. It normally would not be glossy because of its pigment:binder ratio, and even if not porous, would seldom permit sanding or abrasion without showing al readily-apparent blemish where the sanding occurred. It is inferior as an exposed face for these and other reasons, and for architectural appeal and maximum durability should be overlaid with the first-applied gelled layer. Heretofore, however, there was no known way to adhere an overlay to such highly pigmented layer.
  • the overlay 2 and the pigmented backing layer 3 can be applied in registering juxtaposition in an uncuredl state, and then cured simultaneously.
  • the layers are bonded integrally to each other and to the face of the block 4.
  • EXAMPLE 2 in this example, the principles of our invention are exemplified by the preparation of a vehicle license plate in which the main body of the plate is composed of glass-fiber-reinforced, colored, polyester resin, and the numerals and other indicia thereon are composed of pigmented polyester resin of a contrasting color integrally bonded to the body of the plate.
  • the legible face of the plate is to be fiat and smooth; that is, that the numerals and other indicia are ⁇ neither embossed nor engraved with respect. to the plane of the legible face of the plate.
  • a mold l@ is provided in which mold there is a shallow rectangular cavity conforming in horizontal dimensions to the length and width of the desired plate.
  • the cavity terminates in its downward vertical direction in a flat bottom wall or follower plate 11 suitably ground and polished to a smoothness consistent with the smoothness which is desired on the legible face of the finished license plate.
  • a negative stencil having the indicia of the desired plate represented as reverse openings extending entirely through the stencil is disposed on said bottom wall so as to block out all of said wall except that which is exposed through the negative indicia openings of the stencil.
  • thickness and of desired color e, gt, blue
  • the stencil is removed, and the sprayed coating 12 is ⁇ gelled by heating it at 225 F. for l to 3 minutes.
  • the blue coating so sprayed can be formulated as follows:
  • Catalysts of the kinds and amounts used with the tripolyester formulation of Example l are added shortly before the coating is sprayed.
  • a ⁇ coat 13 of differently-c0lored (e. g., orange) polyester resin coating similarly catalyzed is then sprayed over the whole bottom wall and over the blue indicia thereon, the color being that which 1s desired as the background of the license plate.
  • the orange coat can be formulated asfollows:
  • Wallastonite (Ca silicate) 2 lbs. Chrome-yellow, light, C. P f3/16 lb. Chrome-orange, light, C. P 1/3 lb. Polyester A, above 7.5 pints. Polyester C, above 01.5 pint. Benzoyl peroxide catalyst 1% by weight.
  • the finished license plate 16 reveals it to be a tough, flexible, light-weight plate having blue indicia on an orange background with the blue indicia corresponding in reverse to the stencil used in applying the first coating to the bottom wall of the mold cavity.
  • the blue indicia form a smooth planar face with the orange front face of the body and are integrally united with the body.
  • the invention provides a process by which polyester resins can be integrally and permanently bonded to other layers or masses of polyester resin(s) as well as to other materials, the fundamental principle involved being that two or more polyester masses can be juxtaposed in an uncured state when at least one of them is in a gelled condition, and then can be subsequently bonded together during the curing of the masses.
  • the principles can be applied widely in the fabrication of innumerable and diverse products, of which only two are illustrated in the foregoing examples.
  • the second coat can be applied in any desired manner to provide an overall, uniform coat or as a design coat cooperating with the first to present ultimately the desired color patterns.
  • two or more patterned color coats may need to be applied before a reasonable facsimile of a wood pattern has been developed.
  • a third over-all coat may then be needed to fill in the voids of the first two and to complete the pattern and the bonding system by which all o-f the colors become permanently bonded to each other and to the subsequently applied backing.
  • 100% polymerizable polyester liquids can be suitably formulated to be curable to a gelled state in advance of the fully-cured state. Curing of the liquids involves exothermic reactions, which exothermicity tends to accelerate the reactions. If polymerization is uncontrolled, as by the non-use of known polymerization stabilizers and/ or inhibitors, the reactive mass cannot be easily kept from proceeding to its fully cured state, but by including appropriate polymerization stabilizers and/ or inhibitors, the mass can be rendered amenable to a gelling treatment in advance of the iinal curing treatment.
  • gelable polyester masses of the types herein described and illustrated above are 100% polymerizable and are usually mixtures of two or more unsaturated polyester types o1' formulations with ⁇ or without polymerizable ethylenicallyunsaturated monomeric material. Nevertheless, a single polyester type or formulation can be used by itself, just as well. Itis more common, though, to mix two or more different ones together since in this way a few stock resin types or formulations can be maintained and from them a large number of blends can readily be prepared.
  • the stock formulations are commonly distinguished from each ⁇ 8 other on the basis of the rigidity or flexibility of the resins they yield. Thus one might give a flexible resin, another might give a semi-rigid resin, and a third might give a rigid resin.
  • the compositions identified hereinabove as Polyester A, Polyester B and Polyester C correspond in principle with this practice, and their various blends (as in the examples) give cured resinous coatings of various degrees of rigidity, selected for the type of service for which the finished product is intended.
  • the present invention can be practiced in connection with any 100% polymerizable polyester formulation or mixture of formulations which can be gelled in an incompletely cured state.
  • this feature of being gelable without being fully cured can be imparted to any unsaturated polyester mass whether clear or pigmented by incorporating known polymerization catalysts, stabilizers and inhibitors in amounts and proportions which are fixed largely by the particular polymerizable polyester mass at hand.
  • any of the usual pigments, inert fillers and extenders can be used, but it is desirable that they be free of or contain only small amounts of reactive metals such as iron, lead, zinc, etc. and/or their compounds.
  • Inerts of high oil absorption e. g., silicates, silica gel
  • high oil absorption e. g., silicates, silica gel
  • zinc and lead pigments since they tend to stiifen the resulting mass. This stilfening effect is not objectionable in the more fluid, less-highly-pigmented formulations.
  • the following formulations illustrate Without limiting the latitude in pigmentation which can be utilized in formulating gelable 100% polymerizable materials for use in the present invention:
  • the whole intercalated mass can then be cured to a tough lm having a desired pattern incorporated between the opposite faces of the cured lm.
  • Example 3 same catalysts are suitable for use with the formulation of Example 3. In both instances, the catalyst mixture is added at time of application. After being catalyzed, the formulations have a pot life of about 30 minutes. Accordingly, each batch should be used up promptly and before the next batch is catalyzed.
  • the process of making a rigid, reinforced structural unit provided with an exposed, formed and pore-free facing of polyester resin which comprises: providing a mold surface adapted to impart to a coating applied thereon a configuration and texture corresponding to that which is desired on the said exposed facing of said unit, applying on at least a part of said mold surface a gelable, liquid polyester coating as a first coating thereon; gelling said first coating without curing it fully; applying at least one additional and different gelable liquid polyester coating over said rst coat and over any selected portions of said mold surface not previously coated by said first coat, thereby to provide multiple coats on at a rigid, structural backing member which is to form the main body of the desired unit in contact with at least one of said additional coatings while the latter is in an ungelled condition, said Contact extending over the area of said backing member which, in the finished article, is to be faced with polyester resin facing; then curing all polyester ⁇ coatings while maintaining contact with said backing member, thereby bonding said coatings to each other and to said backing member at the
  • said first coating is applied over the Whole of said mold surface, wherein said ungelled subsequent coating is pigmented to provide hiding of said backing member; and wherein said backing member is a preformed building block composed essentially of inorganic material, and is positioned so that one face thereof is substantially completely in contact with said ungelled subsequent coating while it is being fully cured, whereby said building block is integrally bonded over one face thereof to said first and subsequent coatings.

Description

Dec 24, 1957 DQ K. BlcKEL Erm. 2,817,619
PROCESS FOR PREPARING- ROLYESTER-FACED BODIES Filed July 2, 1954 man DAV/0 Y K' Bla/fel.
STEPHEN J- M/rTL INVENTORS ATTY United States Patent David K. Bickel and Stephen J. Mittl, Reading, signors to The Glidden Company, Cleveland, corporation of Ohio Application JulyZ, 1954, Serial No. 441,152
3 Claims. (Cl. 154-110) Pa., as (lhio, a
Thisinvention relates to a process for preparing bodies composed of or comprising a cured polyester resin mass as a backing on the surface of which is integrally attached an exposed or finish layer of clear or pigmented polyester resin. The invention contemplates the provision of either finish layers of a monotone appearance, or finish layers combining two or more different colors or resinous masses in any desired arrangement or pattern.
Various polyester resins (alkyd resins prepared mainly from saturated polyhydric alcohols and ethylenically-unsaturated polycarboxylic acids) and various resinous products which combine polyester resins with polymerizable ethylenically unsaturated monomers are well known compositions of matter, and are well known to possess and exhibit excellent hardness, abrasion resistance, toughness, mar resistance, chemical resistance and Wear resistance, and accordingly are well suited for use as protective finishes for indoor and outdoor exposure. Such resinous compositions are, moreover, excellent binders and molding materials and hence can be used prominently in a wide variety of finished products. When used as a binder for glass fibers and like reinforcing material, molded arti cles of excellent mechanical strength can be produced.
The foregoing advantageous properties of polyesters and polyestenmonomer combinations, however, are beset with one disadvantage in particular; namely, that to the best of the applicants present knowledge, few known paints, inks, or conventional coating compositions other than cer tain lacquers will adhere satisfactorily to the cured surface of such resinous materials. This quality, while advantageous in many respects, is a definite disadvantage from the standpoint of applying markings, legends, insignia, decorations, etc. to cured surfaces of the resins. Thus, such markings as trademarks, trade names, manufacturers name and address, quality or grade designations, and the like cannot be affixed permanently in any simple manner. Moreoven it has not heretofore been possible to make such products as signs, name-plates, license plates and many other products carrying indicia of one sort or another from such resins since the indicia will not adhere to the resins if painted, printed, stencilled, or otherwise conventionally applied thereon.
Poor adherence to the cured surfaces of such resins is also a disadvantage in another direction. Polyester or polyester-monomer resins are currently being used rather extensively in making a variety of reinforced decorative and/or structural materials as automobile bodies, safety helmets, lamp shades, canopy material in corrugated sheet form, light weight bath-tubs for automobile trailers,` and many other objects. in most instances certain of the reinforcing bers are very close to the surface of the finished objects and in some instances may penetratethe surface. lf the surface is sanded in an` effort to out o' the protruding reinforcing fibers the very act of abradingthe surface exposes new fiberswhich` further detract from` thed'esired smooth, pore-free surface. Moreover, each exposed reVw inforcing fiber functions as a wick in leading moisture through the cured mass of polyester. For example, glassiiber-reinforced polyester tubing is not watertight because of the wick action of fibers which penetrate through the inner surface of the tubing.
Our process involves the concept of building up the desired finished body inwardly from the desired smooth, defect-free outer surface, rather than to build it from the inside out, as has heretofore been attempted. By proceeding in this way, the desired outer surface can be pro vided in the form, quality, color and pattern sought, whether that be a liber-free and pore-free surface of a single homogeneous color, a sign` exposing an outer surface of two or more colors, or a decorative surface having an appearance and pattern resembling wood, marble, or otherwise. ln carrying out our concept, the desired outer surface is provided first of all by applying a selected gelable polyester composition to an appropriate mold surface and then is gelled in place on said mold surface without being cured; then a desired polyester mass reinforced or not can be applied on top thereof and in some instances gelled without being fully cured, and then (if desired) structural and/or reinforcing members of metal, stone, rock, concrete or the like can be applied on top of the gelled but uncured mass. The entire assembly so built up can then be treated to cure the various resin layers simultaneously, as by heat alone, or by combinations of heat and pressure, to give a finished body having ail of the various layers and masses integrally united each to another and to any structural members employed therein, thereby to provide a body having a durable, smooth, glossy, abrasionand chemical-resistant outer surface carrying any desired legends, indicia or patterns as an integral part of that outer surface.
Of fundamental importance to the process outlined above is the concept and provision of a polyester or polyester-monomer mass which can be converted in its entirety to a fairly rigid state while yet not being in a fully cured condition. The fairly rigid state, hereinafter referred to as the gel state', permits each layer to be applied and converted to a condition of moderate rigidity before the next layer or mass is laid upon it. After the desired assembly of layers and/or masses has been completed, the entire assembly of gelled resinous masses therein can be further converted to a fully cured and inter-bonded condition. Accordingly, it is an object of the present invention to provide a process wherein intercalated layers of gelled but incompletely cured polyester resin are subsequently integrally bonded together.
It is another object to bond layers and/0r masses of differently colored and/or pigmented polyester resin together, and in the course thereof to produce an outer or exposed surface of cured polyester resin which is smooth, glossy and free of such reinforcing fibers or particles as may be used in layers and/or masses of polyester resin which are integrally united with said outer surface and which reinforce and support the said outer surface.
It is still another object to provide a process for preparing molded objects having a smooth, pore-free outer surface of polyester resin,` which surface carries desired indicia thereinas an integral part of said surface, whereby signs, license plates and other indicia-carrying objectsl can be so fabricated that at least the exposed surface of the object is composed mainly of polyester and/ or polyester` monomer resin( s) These and other objects will be apparent from the following examples of the invention, taken in conjunction with the attached drawings in which:
Fig. l isa vertical longitudinal sectional view of a building block as positioned in a tray for applying a composite facing thereto;
Fig. 2 is a vertical cross-sectional view taken on the line 2 2 of Fig. 1;
Fig. 3 is a plan view of a mold for a license plate. showing identifying characters which have been sprayed on the bottom face of the mold by means of a reverse stencil;
Fig. 4 is a vertical sectional View of the mold of Fig. 4 as taken on the line 4-4 after additional layers of materials have been provided therein, said view having its vertical dimensions greatly enlarged;
Fig. 5 is a plan view of the completed license plate after being ejected from the mold;
Fig. 6 is a plan view of an assembly such as could be prepared in accordance with the invention in making a decorated sheet of polyester foil;
Fig. 7 is a vertical sectional view of the assembly of Fig. 6, taken on the line 7-7 and greatly enlarged in the vertical dimensions.
EXAMPLE l Building black faced with polyester' resin This example illustrates the principles of the invention as applied to the preparation of a faced porous building block whose dimensions are approximately 8" x 8" x 16". From what has been said above, it will be understood that the object of facing the building block is to provide at least one smooth, non-porous, exposure-resistant facing on the block to present any desired color or color pattern. Such faced blocks can be laid up so as to form a wall presenting their resinfaced surfaces either to an inside room of a structure, or to the weather side of the wall. The blocks may, of course, be faced on both sides. Where the facings are exposed to the weather, they provide an exterior surface which needs no painting, which is water-tight, which stays clean by reason of its smoothness and weather resistance, and which is rnar resistant by reason of its toughness, abrasion resistance and hardness. Where the facings are presented to interior rooms of a structure, they alford many of the advantages mentioned above plus ease of cleaning, retention of color, brightness and decorative qualities, excellent durability and a certain degree of fire-resistance. Such a surface seldom needs to be more than a few thousandths of an inch thick but in commercial practice may be as much as 3%000 of an inch thick. Any desired thickness can, of course, be used. Under the just-described outer layer will be a resinous layer which has been pigmented and/or filled or reinforced with appropriate materials, the pigmentation giving a sub-surface layer of desired hiding qualities with the fillers and reinforcement functioning to extend or bulk the resin while yet providing a strong, dense layer capable of adequately supporting the nonporous exposed surface layer. The intermediate layer must of course be firmly bonded both to the exposed surface layer and to the cinder block.
A faced block of the structure just described can be prepared in the following manner, reference being had to Figs. l and 2 of the attached drawings.
The inside surface of a clean metal tray 1 having dimensions of about 8" x 16" in plan view and about l/." deep is sprayed to a thickness of about 5 to l0 mils with a catalyzed 100% polymerizable, gelable resinous polyester mass formulated as follows, thereby to provide a layer 2 in the tray.
Formulation Rutile TiO2 3 lbs. 3 oz. Chrome green (med.) 3 oz. Kieselguhr 2 lbs. l0 oz. Polyester A 77 liquid ounces. Polyester B 32 liquid ounces.
Polyester C liquid ounces.
Polyester A is a liquid heathardeuable polyester composition prepared from the following ingredients:
1Paste.
Polyesters B and C are similar heat-hardenable cornpositions, formulated as indicated below:
Polyester B Lbs. Propylene glycol 29.90 Maleic anhydride 17.50 Adipic acid 26.10 Styrene 27.35 Xylol 5.88 4tertbutyl catechol .009 Choline chloride.l .456 Propylene glycol1 .10
1 Stabilizer paste.
Polyester C Lbs. Diethylene glycol 46.2 Maleic anhydride 19.4 Adipic acid 28.9 Styrene 36.0 f Xy1oi 7.5
4-tert-buty1 catechol .012 Choline chloride .06
These three polyester compositions can be prepared individually by esterifying the polyhydric alcohol(s) and polycarboxylic acids in the presence of xylol as the iirst step, then the volatiles are stripped olf and, after cooling, the stabilizers and styrene are added. The resulting cornpositions are polymerizable.
By adding 1% of methylethylketone peroxide and 1% of 0.2% cobalt naphthenate solution to the tri-polyester formulation, the sprayed coating is converted in a few minutes to a fairly firm gelled condition at room ternperature, and by adding 1% of benzoyl peroxide or 1% methylethylketone peroxide the sprayed layer 2 can be gelled at 225 F. in about 1 to 3 minutes. A suitable backing-and-bonding mass formulated as follows is then added to the tray in an amount of about 1.5 lbs. to form a layer 3.
The mass is catalyzed for curing by incorporating 0.5 %1.0% of methylethylketone peroxide, t-butyl peroxide or benzoyl peroxide.
The above backing-and-bonding mass is a thick, creamy material which can be poured into the tray and spread easily therein. It has enough body to carry the weight of the cinder block Without being squeezed out of the tray. The cinder block 4 is then positioned in the tray with. one face thereof resting upon the layer tional backing-and-bonding material can then be intro-` duced` between the edges of the block and the sides of the tray to completely hide the face which is being coated. The tray with its entire assembly is next passed into an oven where the whole unit isheated at 350 F. for about 45 minutes, thereby curing` the gelled polyester resin layer 2 and the layer 3- of backing-and-bonding mass, and bonding them to each other and to the cinder block. Gn emergence from the oven, the tray 1 can be easily removed from the cured assembly and returned for use in preparing another cured assembly, since the above formulations do not adhere tothe tray after being cured.
The advantages of this process` are:
(l) The first-applied gelled coating 2 cures to a dense, pore-free, smooth surface of desired uniform color and presents the physical and chemical properties of the selected polyester resin as the Wearing face of the block.
(2) The second-applied gelled layer 3v is relatively high in pigment and filler and low in resin content and hence of moderate total cost even though being used" in appreciable volume (e. g., about l.5 lbs. per face) to give hiding, bonding, pore-filling, and leveling-out between the first gelled coat and non-flat block faces. It normally would not be glossy because of its pigment:binder ratio, and even if not porous, would seldom permit sanding or abrasion without showing al readily-apparent blemish where the sanding occurred. It is inferior as an exposed face for these and other reasons, and for architectural appeal and maximum durability should be overlaid with the first-applied gelled layer. Heretofore, however, there was no known way to adhere an overlay to such highly pigmented layer.
(3) By the present process, however, the overlay 2 and the pigmented backing layer 3 can be applied in registering juxtaposition in an uncuredl state, and then cured simultaneously. By such curing treatment, the layers are bonded integrally to each other and to the face of the block 4.
(4) The sequence and conduct of the operations permits blocks` to be faced on a commercial basis with a high yield of merchantable product.
EXAMPLE 2 in this example, the principles of our invention are exemplified by the preparation of a vehicle license plate in which the main body of the plate is composed of glass-fiber-reinforced, colored, polyester resin, and the numerals and other indicia thereon are composed of pigmented polyester resin of a contrasting color integrally bonded to the body of the plate. In this example it is assumed that` the legible face of the plate is to be fiat and smooth; that is, that the numerals and other indicia are` neither embossed nor engraved with respect. to the plane of the legible face of the plate.
One method which can be used to prepare such a license plate is as follows, reference now being made to Figs. 3-5.
A mold l@ is provided in which mold there is a shallow rectangular cavity conforming in horizontal dimensions to the length and width of the desired plate. The cavity terminates in its downward vertical direction in a flat bottom wall or follower plate 11 suitably ground and polished to a smoothness consistent with the smoothness which is desired on the legible face of the finished license plate.
A negative stencil having the indicia of the desired plate represented as reverse openings extending entirely through the stencil is disposed on said bottom wall so as to block out all of said wall except that which is exposed through the negative indicia openings of the stencil. thickness and of desired color (e, gt, blue) is then A polyester resin coating 12 of a few mils in` 6 sprayed on the exposed portionsv of the bottom wall to deposita coating which in color and disposition will constitute the legible numerals and indicia of the finished license plate. The stencil is removed, and the sprayed coating 12 is` gelled by heating it at 225 F. for l to 3 minutes. The blue coating so sprayed can be formulated as follows:
Indanthrene Blue 2 oz. Kieselguhr 1/z lb. Polyester A above 2 lb. l0 oz. Polyester B above 76 liquid oz. Polyester C above 32 liquid oz. Ti02 20 liquid oz; Benzoquinone (1% para, in styrene monomer) 2 liquid oz.
Catalysts of the kinds and amounts used with the tripolyester formulation of Example l are added shortly before the coating is sprayed. After the stencilled coating has been gelled, a` coat 13 of differently-c0lored (e. g., orange) polyester resin coating similarly catalyzed is then sprayed over the whole bottom wall and over the blue indicia thereon, the color being that which 1s desired as the background of the license plate. The orange coat can be formulated asfollows:
The coating is sprayed to a thickness of about 5 to 10i mils and then is gelled by heating at 225 F. for about l to 3 minutes. A catalyzed4 polyester molding resin 14 in liquid form and formulated as follows:
Wallastonite (Ca silicate) 2 lbs. Chrome-yellow, light, C. P f3/16 lb. Chrome-orange, light, C. P 1/3 lb. Polyester A, above 7.5 pints. Polyester C, above 01.5 pint. Benzoyl peroxide catalyst 1% by weight.
and` a preformed mat 15 of glass-fiber are introduced into the cavity on top of the second gelled coat 13, and then the entire contents of the cavity is pressed under a pressure of about 20 lbs. per square inch for l to 4 minutes at 225 F., thereby to mold the resin and glass-fiber into the form of the main body of the license plate, and simultaneously to cure and bond the various layers of polyester resin into` an integral unit. T he cured assembly can then be ejected from the mold. Examination of the finished license plate 16 reveals it to be a tough, flexible, light-weight plate having blue indicia on an orange background with the blue indicia corresponding in reverse to the stencil used in applying the first coating to the bottom wall of the mold cavity. The blue indicia form a smooth planar face with the orange front face of the body and are integrally united with the body.
From the foregoing examples it will be clear that the invention provides a process by which polyester resins can be integrally and permanently bonded to other layers or masses of polyester resin(s) as well as to other materials, the fundamental principle involved being that two or more polyester masses can be juxtaposed in an uncured state when at least one of them is in a gelled condition, and then can be subsequently bonded together during the curing of the masses. The principles can be applied widely in the fabrication of innumerable and diverse products, of which only two are illustrated in the foregoing examples.
Whilethe examples have illustrated the application of the tirstor exterior-coat to a molding surface by spraying,
7 other conventional method-s of application can of course be used,`as by brushing, by silk screening, roller coating, printing, etc. so that designs of any desired simplicity or complexity can be applied by appropriate methods and apparatus. In like manner, the second coat can be applied in any desired manner to provide an overall, uniform coat or as a design coat cooperating with the first to present ultimately the desired color patterns. Thus, where a grained pattern resembling wood grain is desired, two or more patterned color coats may need to be applied before a reasonable facsimile of a wood pattern has been developed. A third over-all coat may then be needed to fill in the voids of the first two and to complete the pattern and the bonding system by which all o-f the colors become permanently bonded to each other and to the subsequently applied backing. Various other ways of adapting the principles of our invention to particular ornamenting and/ or legend aixing situations will be apparent to those skilled in the art.
It will be appreciated that in carrying out the principles of our invention, one can use any of a large number of known resin or resin mixtures of the types commonly referred to as unsaturated polyesters. The latter term used here as above to mean resinifiable masses containing or composed of organic polycarboxylic acid esters which are polymerizable mainly by reason of ethylenic unsaturation in the polycarboxylic acid radicals and which are employed either by themselves or in combination with polymerizable ethylenically-unsaturated compounds (e. g., styrene) usually in monomeric or low-polymer form. should be understood, however, that such unsaturated polyester resins need not be free or saturated polyesters or other heat-convertible modifying resins, and that various modifying polymerizable, saturated polyester resins or convertible resinous masses (e. g., alkyds) can be used in minor to prominent amounts therein. It should also be understood that the unsaturated polyesters and/ or mixtures of saturated and unsaturated polyesters can be modified in a variety of other ways well known to those skilled in the art. The following patent specifications are referred to as indicating the scope of the unsaturated polyester resin art which can be employed in practicing the principles of our invention: U. S. Patents 2,512,410, 2,593,787, 2,280,256, 2,453,666, 2,443,736, 2,443,737, 2,409,633, 2,610,168 2,635,089 and the copending application-s Ser. No. 307,703, filed September 3, 1952, now abandoned, and Ser. No. 377,265, tiled August 28, i953, now Patent No. 2,777,829.
It is well known to those skilled in the unsaturated polyester resin art that 100% polymerizable polyester liquids can be suitably formulated to be curable to a gelled state in advance of the fully-cured state. Curing of the liquids involves exothermic reactions, which exothermicity tends to accelerate the reactions. If polymerization is uncontrolled, as by the non-use of known polymerization stabilizers and/ or inhibitors, the reactive mass cannot be easily kept from proceeding to its fully cured state, but by including appropriate polymerization stabilizers and/ or inhibitors, the mass can be rendered amenable to a gelling treatment in advance of the iinal curing treatment. The examples illustrate the use of inhibitors, stabilizers and pigmentation to control the reactivity so that the desired gelled but uncured state can be attained controllably in advance of the fully cured state. In general, gelable polyester masses of the types herein described and illustrated above are 100% polymerizable and are usually mixtures of two or more unsaturated polyester types o1' formulations with `or without polymerizable ethylenicallyunsaturated monomeric material. Nevertheless, a single polyester type or formulation can be used by itself, just as well. Itis more common, though, to mix two or more different ones together since in this way a few stock resin types or formulations can be maintained and from them a large number of blends can readily be prepared. The stock formulations are commonly distinguished from each `8 other on the basis of the rigidity or flexibility of the resins they yield. Thus one might give a flexible resin, another might give a semi-rigid resin, and a third might give a rigid resin. The compositions identified hereinabove as Polyester A, Polyester B and Polyester C correspond in principle with this practice, and their various blends (as in the examples) give cured resinous coatings of various degrees of rigidity, selected for the type of service for which the finished product is intended. Tho-se skilled in the art of formulating unsaturated polyester resins recognize that the proportions of saturated carboxylic acids to 0:,[3 unsaturated carboxylic acids, the length of the carbon chain(s) involved in the carboxylic acids and in the polyhydrie alcohols, the proportion of polyester to polymerizable unsaturated monomer (if any), the type of ethylenic monomer, the degree of functionality in the carboxylic acids and polyhydric alcohols, and the curing treatment(s), are all factors affecting the flexibility and/or rigidity of the cured resin. Since such knowledge is now known and has been long used by those skilled in the art, and is only an incidental feature in the present invention, no extended discussion of such formulation details seems necessary to enable a person skilled in the art to practice the present invention. In principle, the present invention can be practiced in connection with any 100% polymerizable polyester formulation or mixture of formulations which can be gelled in an incompletely cured state. As those skilled in the art are aware, this feature of being gelable without being fully cured can be imparted to any unsaturated polyester mass whether clear or pigmented by incorporating known polymerization catalysts, stabilizers and inhibitors in amounts and proportions which are fixed largely by the particular polymerizable polyester mass at hand. When that mass is pigmented, particularly with amounts and kinds of pigment which in the aggregate possess what is known in the art as high oil absorption, then a wholly different combination (i. e., kinds and/or amounts) of polymerization catalysts, stabilizers and inhibitors is apt to be needed than if the same polyester mass without any pigment therein were being formulated to secure the quality of gelability without full curing. For most purposes of the present invention, however, unpigmented gelable polyester coatings are apt to be of minor importance since the gelable coatings are usually desired for their hiding, extending and/ or color-imparting qualities. Hence hiding and/or color pigment-s are usually included. Any of the usual pigments, inert fillers and extenders can be used, but it is desirable that they be free of or contain only small amounts of reactive metals such as iron, lead, zinc, etc. and/or their compounds. Inerts of high oil absorption (e. g., silicates, silica gel) are preferred, only enough high-hiding pigment being used to serve the purpose at hand. In highly pigmented gelable polyester masses, it is desirable to exclude zinc and lead pigments since they tend to stiifen the resulting mass. This stilfening effect is not objectionable in the more fluid, less-highly-pigmented formulations. The following formulations illustrate Without limiting the latitude in pigmentation which can be utilized in formulating gelable 100% polymerizable materials for use in the present invention:
EXAMPLE 3 Pints PolyesterA 6.75 PolyesterB .75 PolyesterC 2.50
`tion on a support 21 as shown in Figs. 6 and 7, gelling it,
then applying a colored polyester pattern layer 22 thereon,
9 and finally applying one or more subsequent clear layers 23. The whole intercalated mass can then be cured to a tough lm having a desired pattern incorporated between the opposite faces of the cured lm.
EXAMPLE 4 PolyesterA 4 gals., 45 fl. ozs. PolyesterC 3 gals., 77 ozs. Magnesium silicate .124 lbs., 3 ozs. White talc 124 lbs., 3 ozs. Tio2 -2 1 1b.
same catalysts are suitable for use with the formulation of Example 3. In both instances, the catalyst mixture is added at time of application. After being catalyzed, the formulations have a pot life of about 30 minutes. Accordingly, each batch should be used up promptly and before the next batch is catalyzed.
The numerous patents identified hereinabove exemplify not only the scope of the polyester formulations which we contemplate as being part of this invention, but also illustrate and describe some of the numerous polymerization catalysts, stabilizers and inhibitors which are known to be useful in such formulations. The catalysts of Examples 3 and 4 can be replaced with many other catalyst combinations of the types and kinds known to those skilled in the art.
3 Having now described our invention, what we claim 1s:
l. The process of making a rigid, reinforced structural unit provided with an exposed, formed and pore-free facing of polyester resin which comprises: providing a mold surface adapted to impart to a coating applied thereon a configuration and texture corresponding to that which is desired on the said exposed facing of said unit, applying on at least a part of said mold surface a gelable, liquid polyester coating as a first coating thereon; gelling said first coating without curing it fully; applying at least one additional and different gelable liquid polyester coating over said rst coat and over any selected portions of said mold surface not previously coated by said first coat, thereby to provide multiple coats on at a rigid, structural backing member which is to form the main body of the desired unit in contact with at least one of said additional coatings while the latter is in an ungelled condition, said Contact extending over the area of said backing member which, in the finished article, is to be faced with polyester resin facing; then curing all polyester `coatings while maintaining contact with said backing member, thereby bonding said coatings to each other and to said backing member at the respective points of contact of each with another; and finally removing the cured and bonded assembly from contact with said mold surface, said liquid polyester coatings being (l) polyhydric alcohol-polycarboxylic acid ester products characterized by original ethylenic unsaturation in at least some of the polycarboxylic acid radicals, and being (2) substantially 100% polymerizable to a gel state in advance of the fully-cured state.
2. The process as claimed in claim 1 wherein said first coating is applied over the Whole of said mold surface, wherein said ungelled subsequent coating is pigmented to provide hiding of said backing member; and wherein said backing member is a preformed building block composed essentially of inorganic material, and is positioned so that one face thereof is substantially completely in contact with said ungelled subsequent coating while it is being fully cured, whereby said building block is integrally bonded over one face thereof to said first and subsequent coatings.
3. The process as claimed in claim 1 wherein said rst coating is applied in a predetermined pattern over only a portion of said mold surface; wherein at least one subsequent coating of different appearance when cured covers any voids on said mold surface left uncoated by previous coatings and is gelled without complete curing before any subsequent materials are brought into contact with it; the finished article carries a pattern in its exposed face corresponding to the pattern in which said first coating was applied to said mold surface.
References Cited in the le of this patent UNITED STATES PATENTS OTHER REFERENCES Tailor-made Polyester Resin Modern Plastics, Oc-
tober 1947, pages 111-115, page 111 particularly relied on.

Claims (1)

1. THE PROCESS OF MAKING A RIGID, REINFORCED STRUCTURAL UNIT PROVIDED WITH AN EXPOSED, FORMED AND PORE-FREE FACING OF POLYESTER RESIN WHICH COMPRISES: PROVIDING A MOLD SURFACE ADAPTED TO IMPART TO A COATING APPLIED THEREON A CONFIGURATION AND TEXTURE CORRESPONDING TO THAT WHICH IS DESIRED ON THE SAID EXPOSED FACING OF SAID UNIT, APPLYING ON AT LEAST A PART OF SAID MOLD SURFACE A GELABLE, LIQUID POLYESTER COATING AS A FIRST COATING THEREON; GELLING SAID FIRST COATING WITHOUT CURING IT FULLY; APPLYING AT LEAST ONE ADDITIONAL AND DIFFERENT GELABLE LIQUID POLYESTER COATING OVER SAID FIRST COAT AND OVER ANY SELECTED PORTIONS OF SAID MOLD SURFACE NOT PREVIOUSLY COATED BY SAID FIRST COAT, THEREBY TO PROVIDE MULTIPLE COATS ON AT LEAST SELECTED PORTIONS OF SAID MOLD SURFACE; POSITIONING A RIGID, STRUCTURAL BACKING MEMBER WHICH IS TO FORM THE MAIN BODY OF THE DESIRED UNIT IN CONTACT WITH AT LEAST ONE OF SAID ADDITIONAL COATINGS WHILE THE LATTER IS IN AN
US441152A 1954-07-02 1954-07-02 Process for preparing polyester-faced bodies Expired - Lifetime US2817619A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US441152A US2817619A (en) 1954-07-02 1954-07-02 Process for preparing polyester-faced bodies

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US441152A US2817619A (en) 1954-07-02 1954-07-02 Process for preparing polyester-faced bodies

Publications (1)

Publication Number Publication Date
US2817619A true US2817619A (en) 1957-12-24

Family

ID=23751751

Family Applications (1)

Application Number Title Priority Date Filing Date
US441152A Expired - Lifetime US2817619A (en) 1954-07-02 1954-07-02 Process for preparing polyester-faced bodies

Country Status (1)

Country Link
US (1) US2817619A (en)

Cited By (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2905580A (en) * 1955-10-21 1959-09-22 Jr George J Kreier Method for making color-patterned glass fiber sheet
US2951001A (en) * 1956-01-12 1960-08-30 Rubenstein David Decorative structural element
US2965532A (en) * 1955-05-20 1960-12-20 Fmc Corp Method for manufacturing resin coated glass-reinforced plastics and product
US3027290A (en) * 1958-03-13 1962-03-27 Texas Industries Inc Composite building unit and method for making same
US3030234A (en) * 1958-04-02 1962-04-17 Burns & Russell Co Filled polyester resin having a coating of epoxy resin and method of manufacturing the same
US3051585A (en) * 1958-12-02 1962-08-28 Hooker Chemical Corp Protective coatings for polyester resins
US3061500A (en) * 1960-04-01 1962-10-30 Jr George J Kreier Method of making plastic bas-reliefs
US3082134A (en) * 1958-07-10 1963-03-19 Specialties Dev Corp Hollow articles and method of making the same
US3089784A (en) * 1960-03-24 1963-05-14 Diamond Alkali Co Polyester coating system
US3124626A (en) * 1964-03-10 Process for producing boat hulls of sandwich construction
US3129110A (en) * 1958-07-31 1964-04-14 Glidden Co Process of producing decorative plastic surfaces
US3135625A (en) * 1958-08-29 1964-06-02 Masonite Corp Method for applying catalyzed coating compositions
US3150032A (en) * 1956-06-25 1964-09-22 Rubenstein David Abuse resistant articles of manufacture and method of making
US3193435A (en) * 1961-08-16 1965-07-06 Freeman Chemical Corp Laminated articles having deeply embossed surfaces and method of making same
US3194679A (en) * 1957-06-05 1965-07-13 Glidden Co Polyester coatings
US3207645A (en) * 1960-05-09 1965-09-21 Rhone Poulenc Sa Process for the preparation of laminar structure consisting of polystyrene and polyester
US3240619A (en) * 1960-06-21 1966-03-15 Interchem Corp Method of coating with polyester resins
US3242027A (en) * 1954-10-06 1966-03-22 Gladwin Plastics Inc Methods of producing molded articles
US3255061A (en) * 1962-04-20 1966-06-07 Us Rubber Co Process for making synthetic leather-like material
US3272645A (en) * 1959-09-29 1966-09-13 Houilleres Bassin Du Nord Moldable laminated sheet materials and method of making same
US3284262A (en) * 1960-03-24 1966-11-08 Diamond Alkali Co Process of applying a polyester coating to a reinforced, coated substrate
US3309254A (en) * 1961-02-03 1967-03-14 Rowe James Walker Process for transfer of ink or dye printed images to epoxy resin surfaces
US3312761A (en) * 1963-03-07 1967-04-04 Vida Alex Method of making building facing material
US3320341A (en) * 1960-02-24 1967-05-16 William L Mackie Method of manufacturing a lightweight microwave antenna
US3322609A (en) * 1963-03-07 1967-05-30 Vida Alex Building facing material
US3328231A (en) * 1966-04-13 1967-06-27 Burns & Russell Co Method of producing cast surfaces and product obtained thereby
US3330079A (en) * 1964-09-21 1967-07-11 John W Mitchell Building block
US3340115A (en) * 1957-12-11 1967-09-05 Rubenstein David Method of making a reinforced composite concrete pipe
US3351510A (en) * 1964-07-07 1967-11-07 Armstrong Cork Co Method of making sheet material
US3379592A (en) * 1962-09-12 1968-04-23 Ostrowicz Joel Decoration of thermoset plastics
US3379603A (en) * 1959-04-24 1968-04-23 Barnette Stanley Ronald Cast plastic laminates and cast plastic articles of manufacture
US3454692A (en) * 1965-03-11 1969-07-08 Donnelly Mirrors Inc Method of forming vehicular rearview mirrors
US3476628A (en) * 1966-07-15 1969-11-04 Frederick W Cronin Method of preparing surfaced panels
US3518146A (en) * 1966-03-25 1970-06-30 Marvin E Plympton Method of making simulated inlaid designs
US3619457A (en) * 1968-09-20 1971-11-09 Thermoform Plastics Inc Method of forming structural units
US3772051A (en) * 1971-07-29 1973-11-13 Ici Ltd Decorative flooring surfaces
US3799717A (en) * 1972-04-11 1974-03-26 A Nedoh Apparatus for applying, attaching and processing decorative facing to an article
US3855027A (en) * 1972-06-22 1974-12-17 Itt On-site fabrication of antennas
US4031289A (en) * 1976-05-11 1977-06-21 The Burns & Russell Company Of Baltimore City Stain resistant polyester-coated block
US4209486A (en) * 1979-02-05 1980-06-24 Ross Wallace D Process of inlaying a design in molded simulated marble
US4244993A (en) * 1979-07-10 1981-01-13 P & G Products, Inc. Method for making simulated marble and product of the method
US4499142A (en) * 1983-03-31 1985-02-12 Trenwyth Industris, Inc. Faced masonry units and facing composition therefor
US4553364A (en) * 1982-12-23 1985-11-19 Owens-Corning Fiberglas Corporation Window sash and frame molded of fibrous material
US4643789A (en) * 1982-07-23 1987-02-17 Transfer Print Foils Method for preparing a decorated insert and continuous insert molding operation
WO1994021476A1 (en) * 1993-03-23 1994-09-29 Akbar Ghahary Decorative facings for bricks and cinderblocks
US5648030A (en) * 1995-02-01 1997-07-15 Dagger, Inc. Method for obtaining high definition graphics in surfaces of molded plastic objects
US5913791A (en) * 1997-05-08 1999-06-22 Baldwin; Robert A. Building block, method for making the same, and method for building a wall using the same
US20020112427A1 (en) * 1997-05-08 2002-08-22 Baldwin Robert A. Building block with a cement-based attachment layer
US20120291391A1 (en) * 2007-06-21 2012-11-22 Keystone Retaining Wall Systems Llc Veneers for walls, retaining walls, retaining wall blocks, and the like

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1678613A (en) * 1926-07-22 1928-07-24 Weiss Albert Method and apparatus for making building blocks
US2330400A (en) * 1937-09-11 1943-09-28 American Anode Inc Method of making distensible bag catheters and the like
US2459279A (en) * 1947-06-24 1949-01-18 Laminating Specialties Inc Process for plastic coating
US2495640A (en) * 1946-05-31 1950-01-24 Method of molding
US2545832A (en) * 1945-08-27 1951-03-20 Shell Dev Method for manufacturing laminated articles
US2614955A (en) * 1950-01-13 1952-10-21 L A Darling Company Pressure molding laminates
US2695256A (en) * 1952-11-12 1954-11-23 Carl A Strand Lightweight bathtub and production thereof
US2751775A (en) * 1955-07-12 1956-06-26 Burns & Russell Co Masonry block having an integral molded facing layer and method of making same
US2752275A (en) * 1952-09-05 1956-06-26 Burns And Russell Company Surface finished masonry construction unit

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1678613A (en) * 1926-07-22 1928-07-24 Weiss Albert Method and apparatus for making building blocks
US2330400A (en) * 1937-09-11 1943-09-28 American Anode Inc Method of making distensible bag catheters and the like
US2545832A (en) * 1945-08-27 1951-03-20 Shell Dev Method for manufacturing laminated articles
US2495640A (en) * 1946-05-31 1950-01-24 Method of molding
US2459279A (en) * 1947-06-24 1949-01-18 Laminating Specialties Inc Process for plastic coating
US2614955A (en) * 1950-01-13 1952-10-21 L A Darling Company Pressure molding laminates
US2752275A (en) * 1952-09-05 1956-06-26 Burns And Russell Company Surface finished masonry construction unit
US2695256A (en) * 1952-11-12 1954-11-23 Carl A Strand Lightweight bathtub and production thereof
US2751775A (en) * 1955-07-12 1956-06-26 Burns & Russell Co Masonry block having an integral molded facing layer and method of making same

Cited By (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3124626A (en) * 1964-03-10 Process for producing boat hulls of sandwich construction
US3242027A (en) * 1954-10-06 1966-03-22 Gladwin Plastics Inc Methods of producing molded articles
US2965532A (en) * 1955-05-20 1960-12-20 Fmc Corp Method for manufacturing resin coated glass-reinforced plastics and product
US2905580A (en) * 1955-10-21 1959-09-22 Jr George J Kreier Method for making color-patterned glass fiber sheet
US2951001A (en) * 1956-01-12 1960-08-30 Rubenstein David Decorative structural element
US3150032A (en) * 1956-06-25 1964-09-22 Rubenstein David Abuse resistant articles of manufacture and method of making
US3194679A (en) * 1957-06-05 1965-07-13 Glidden Co Polyester coatings
US3340115A (en) * 1957-12-11 1967-09-05 Rubenstein David Method of making a reinforced composite concrete pipe
US3027290A (en) * 1958-03-13 1962-03-27 Texas Industries Inc Composite building unit and method for making same
US3030234A (en) * 1958-04-02 1962-04-17 Burns & Russell Co Filled polyester resin having a coating of epoxy resin and method of manufacturing the same
US3082134A (en) * 1958-07-10 1963-03-19 Specialties Dev Corp Hollow articles and method of making the same
US3129110A (en) * 1958-07-31 1964-04-14 Glidden Co Process of producing decorative plastic surfaces
US3135625A (en) * 1958-08-29 1964-06-02 Masonite Corp Method for applying catalyzed coating compositions
US3051585A (en) * 1958-12-02 1962-08-28 Hooker Chemical Corp Protective coatings for polyester resins
US3379603A (en) * 1959-04-24 1968-04-23 Barnette Stanley Ronald Cast plastic laminates and cast plastic articles of manufacture
US3272645A (en) * 1959-09-29 1966-09-13 Houilleres Bassin Du Nord Moldable laminated sheet materials and method of making same
US3320341A (en) * 1960-02-24 1967-05-16 William L Mackie Method of manufacturing a lightweight microwave antenna
US3089784A (en) * 1960-03-24 1963-05-14 Diamond Alkali Co Polyester coating system
US3284262A (en) * 1960-03-24 1966-11-08 Diamond Alkali Co Process of applying a polyester coating to a reinforced, coated substrate
US3061500A (en) * 1960-04-01 1962-10-30 Jr George J Kreier Method of making plastic bas-reliefs
US3207645A (en) * 1960-05-09 1965-09-21 Rhone Poulenc Sa Process for the preparation of laminar structure consisting of polystyrene and polyester
US3240619A (en) * 1960-06-21 1966-03-15 Interchem Corp Method of coating with polyester resins
US3309254A (en) * 1961-02-03 1967-03-14 Rowe James Walker Process for transfer of ink or dye printed images to epoxy resin surfaces
US3193435A (en) * 1961-08-16 1965-07-06 Freeman Chemical Corp Laminated articles having deeply embossed surfaces and method of making same
US3255061A (en) * 1962-04-20 1966-06-07 Us Rubber Co Process for making synthetic leather-like material
US3379592A (en) * 1962-09-12 1968-04-23 Ostrowicz Joel Decoration of thermoset plastics
US3322609A (en) * 1963-03-07 1967-05-30 Vida Alex Building facing material
US3312761A (en) * 1963-03-07 1967-04-04 Vida Alex Method of making building facing material
US3351510A (en) * 1964-07-07 1967-11-07 Armstrong Cork Co Method of making sheet material
US3330079A (en) * 1964-09-21 1967-07-11 John W Mitchell Building block
US3454692A (en) * 1965-03-11 1969-07-08 Donnelly Mirrors Inc Method of forming vehicular rearview mirrors
US3518146A (en) * 1966-03-25 1970-06-30 Marvin E Plympton Method of making simulated inlaid designs
US3328231A (en) * 1966-04-13 1967-06-27 Burns & Russell Co Method of producing cast surfaces and product obtained thereby
US3476628A (en) * 1966-07-15 1969-11-04 Frederick W Cronin Method of preparing surfaced panels
US3619457A (en) * 1968-09-20 1971-11-09 Thermoform Plastics Inc Method of forming structural units
US3772051A (en) * 1971-07-29 1973-11-13 Ici Ltd Decorative flooring surfaces
US3799717A (en) * 1972-04-11 1974-03-26 A Nedoh Apparatus for applying, attaching and processing decorative facing to an article
US3855027A (en) * 1972-06-22 1974-12-17 Itt On-site fabrication of antennas
US4031289A (en) * 1976-05-11 1977-06-21 The Burns & Russell Company Of Baltimore City Stain resistant polyester-coated block
US4209486A (en) * 1979-02-05 1980-06-24 Ross Wallace D Process of inlaying a design in molded simulated marble
US4244993A (en) * 1979-07-10 1981-01-13 P & G Products, Inc. Method for making simulated marble and product of the method
US4643789A (en) * 1982-07-23 1987-02-17 Transfer Print Foils Method for preparing a decorated insert and continuous insert molding operation
US4553364A (en) * 1982-12-23 1985-11-19 Owens-Corning Fiberglas Corporation Window sash and frame molded of fibrous material
US4499142A (en) * 1983-03-31 1985-02-12 Trenwyth Industris, Inc. Faced masonry units and facing composition therefor
WO1994021476A1 (en) * 1993-03-23 1994-09-29 Akbar Ghahary Decorative facings for bricks and cinderblocks
US5465544A (en) * 1993-03-23 1995-11-14 Safas Corporation Decorative facings for bricks, cinderblocks and the like
US5648030A (en) * 1995-02-01 1997-07-15 Dagger, Inc. Method for obtaining high definition graphics in surfaces of molded plastic objects
US5913791A (en) * 1997-05-08 1999-06-22 Baldwin; Robert A. Building block, method for making the same, and method for building a wall using the same
US20020112427A1 (en) * 1997-05-08 2002-08-22 Baldwin Robert A. Building block with a cement-based attachment layer
US6851235B2 (en) * 1997-05-08 2005-02-08 Robert A. Baldwin Building block with a cement-based attachment layer
US20120291391A1 (en) * 2007-06-21 2012-11-22 Keystone Retaining Wall Systems Llc Veneers for walls, retaining walls, retaining wall blocks, and the like

Similar Documents

Publication Publication Date Title
US2817619A (en) Process for preparing polyester-faced bodies
US4490410A (en) Method of affixing a decorative pattern to a stock or a molded component
CA1198256A (en) Reinforced plastic product
US2752275A (en) Surface finished masonry construction unit
JP4917774B2 (en) Wood-covered composite and method for producing the same
US6150009A (en) Decorative structural panel
US4219598A (en) Molded article, the method for manufacturing the same and the dies therefor
JPH0366126B2 (en)
JP3826267B2 (en) FIBER-REINFORCED PLASTIC MOLDED PRODUCT, ITS MANUFACTURING METHOD, AND MOLDING MOLD USING THE SAME
US20050055931A1 (en) Stones-like laminates
US20080093017A1 (en) Warp-free decorative article of manufacture and method of making same
JP3416528B2 (en) Patterned bathtub and method of manufacturing the same
JPH0716850A (en) Production of artificial stone decorative panel
US3975561A (en) Photopolymer image inlays
JPS58136413A (en) Preparation of molded product with picture pattern
JPS6241472B2 (en)
JPS6228750B2 (en)
JP4917773B2 (en) Wood-covered composite and method for producing the same
JPH0118856B2 (en)
JPH05318468A (en) Gelcoat sheet for molding and preparation thereof and preparation of molding with gelcoat layer using said gelcoat sheet for molding
JP2000301895A (en) Transfer sheet
JPH08174581A (en) Manufacture of decorated molding item
JPS58136411A (en) Preparation of molded product with pattern
JPS5882708A (en) Manufacture of patterned hydrated cured body
JPS62103114A (en) Manufacture of panel